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Cramer Tape Remover 201033

by Cramer Products, Inc.

Cramer Tape Remover 201033 is a Class I device made by Cramer Products, Inc., listed in FDA GUDID since 1 Oct 2018 (UDI-DI 00311960439091), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00311960439091 UDI-DI Date1 Oct 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Cramer Tape Remover
Generic name
Patient medical adhesive remover
Model / reference
201033
Primary DI / UDI-DI
00311960439091
FDA product code
KOX
GMDN term
Patient medical adhesive remover
Device class
Class I
Regulation number
878.4730
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 16 Fluid Ounce

Related devices

Category: Patient medical adhesive remover

Similar devices in this category

Other devices filed under Patient medical adhesive remover.

Other devices from Cramer Products, Inc.

See all devices from Cramer Products, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)